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BMC Musculoskeletal Disorders
|
March 18, 2014
Comparison of orthopaedic manifestations of multiple epiphyseal dysplasia caused by MATN3 versus COMP mutations: a case control study
Sang Gyo Seo, Hae-Ryong Song, Hyun Woo Kim, et al.
European Journal of Medical Genetics
|
December 28, 2014
Case of mild Schmid-type metaphyseal chondrodysplasia with novel sequence variation involving an unusual mutational site of the COL10A1 gene
Hyunwoong Park, Susie Hong, Sung Im Cho, et al.
Clinics in Orthopedic Surgery
|
September 2, 2014
Incidental findings on knee radiographs in children and adolescents
Sang Gyo Seo, Ki Hyuk Sung, Chin Youb Chung, et al.
Clinics in Orthopedic Surgery
|
September 7, 2013
Incidence patterns of pediatric and adolescent orthopaedic fractures according to age groups and seasons in South Korea: a population-based study
Moon Seok Park, Chin Youb Chung, In Ho Choi, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
June 17, 2014
Neurofibromin deficiency-associated transcriptional dysregulation suggests a novel therapy for tibial pseudoarthrosis in NF1
Nandina Paria, Tae-Joon Cho, In Ho Choi, et al.
Journal of Clinical Microbiology
|
January 7, 2005
Detection and identification of Mycobacterium tuberculosis in joint biopsy specimens by rpoB PCR cloning and sequencing
Yeo-Jun Yun, Keun-Hwa Lee, Lin Haihua, et al.
Nature Genetics
|
April 28, 2006
A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva
Eileen M Shore, Meiqi Xu, George J Feldman, et al.
American Journal of Human Genetics
|
August 7, 2012
A single recurrent mutation in the 5'-UTR of IFITM5 causes osteogenesis imperfecta type V
Tae-Joon Cho, Kyung-Eun Lee, Sook-Kyung Lee, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 25, 2015
Comprehensive genetic exploration of skeletal dysplasia using targeted exome sequencing
Jun-Seok Bae, Nayoung K D Kim, Chung Lee, et al.
American Journal of Medical Genetics. Part A
|
October 4, 2011
Revisit of multiple epiphyseal dysplasia: ethnic difference in genotypes and comparison of radiographic features linked to the COMP and MATN3 genes
Ok-Hwa Kim, Hyunwoong Park, Moon-Woo Seong, et al.
Page
of 22
Search research articles
Search
Showing results (201-210 of 211) with videos related to
Sort By:
Page
of 22
BMC Musculoskeletal Disorders
|
March 18, 2014
Comparison of orthopaedic manifestations of multiple epiphyseal dysplasia caused by MATN3 versus COMP mutations: a case control study
Sang Gyo Seo, Hae-Ryong Song, Hyun Woo Kim, et al.
European Journal of Medical Genetics
|
December 28, 2014
Case of mild Schmid-type metaphyseal chondrodysplasia with novel sequence variation involving an unusual mutational site of the COL10A1 gene
Hyunwoong Park, Susie Hong, Sung Im Cho, et al.
Clinics in Orthopedic Surgery
|
September 2, 2014
Incidental findings on knee radiographs in children and adolescents
Sang Gyo Seo, Ki Hyuk Sung, Chin Youb Chung, et al.
Clinics in Orthopedic Surgery
|
September 7, 2013
Incidence patterns of pediatric and adolescent orthopaedic fractures according to age groups and seasons in South Korea: a population-based study
Moon Seok Park, Chin Youb Chung, In Ho Choi, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
June 17, 2014
Neurofibromin deficiency-associated transcriptional dysregulation suggests a novel therapy for tibial pseudoarthrosis in NF1
Nandina Paria, Tae-Joon Cho, In Ho Choi, et al.
Journal of Clinical Microbiology
|
January 7, 2005
Detection and identification of Mycobacterium tuberculosis in joint biopsy specimens by rpoB PCR cloning and sequencing
Yeo-Jun Yun, Keun-Hwa Lee, Lin Haihua, et al.
Nature Genetics
|
April 28, 2006
A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva
Eileen M Shore, Meiqi Xu, George J Feldman, et al.
American Journal of Human Genetics
|
August 7, 2012
A single recurrent mutation in the 5'-UTR of IFITM5 causes osteogenesis imperfecta type V
Tae-Joon Cho, Kyung-Eun Lee, Sook-Kyung Lee, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 25, 2015
Comprehensive genetic exploration of skeletal dysplasia using targeted exome sequencing
Jun-Seok Bae, Nayoung K D Kim, Chung Lee, et al.
American Journal of Medical Genetics. Part A
|
October 4, 2011
Revisit of multiple epiphyseal dysplasia: ethnic difference in genotypes and comparison of radiographic features linked to the COMP and MATN3 genes
Ok-Hwa Kim, Hyunwoong Park, Moon-Woo Seong, et al.
Page
of 22